US4704482A - Catalytic purification of tertiary butyl alcohol - Google Patents
Catalytic purification of tertiary butyl alcohol Download PDFInfo
- Publication number
- US4704482A US4704482A US06/879,660 US87966086A US4704482A US 4704482 A US4704482 A US 4704482A US 87966086 A US87966086 A US 87966086A US 4704482 A US4704482 A US 4704482A
- Authority
- US
- United States
- Prior art keywords
- catalyst
- tertiary butyl
- copper
- nickel
- iron
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 title claims abstract description 75
- 230000003197 catalytic effect Effects 0.000 title description 7
- 238000000746 purification Methods 0.000 title description 2
- 239000003054 catalyst Substances 0.000 claims abstract description 160
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 118
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 77
- 229910052802 copper Inorganic materials 0.000 claims abstract description 63
- 239000010949 copper Substances 0.000 claims abstract description 63
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 59
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 claims abstract description 58
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims abstract description 56
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 53
- 229910052742 iron Inorganic materials 0.000 claims abstract description 43
- 238000006243 chemical reaction Methods 0.000 claims abstract description 39
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000000446 fuel Substances 0.000 claims abstract description 16
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 11
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 10
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 50
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 39
- 238000011109 contamination Methods 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 38
- 229910052804 chromium Inorganic materials 0.000 claims description 31
- 239000011651 chromium Substances 0.000 claims description 31
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 29
- 229910052751 metal Inorganic materials 0.000 claims description 22
- 239000002184 metal Substances 0.000 claims description 22
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 19
- 150000002739 metals Chemical class 0.000 claims description 18
- 230000002708 enhancing effect Effects 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 abstract description 23
- 239000000047 product Substances 0.000 abstract description 13
- 150000002978 peroxides Chemical class 0.000 abstract description 12
- 239000007795 chemical reaction product Substances 0.000 abstract description 6
- 239000000356 contaminant Substances 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 description 28
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 24
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 18
- 230000009467 reduction Effects 0.000 description 15
- 238000006722 reduction reaction Methods 0.000 description 15
- 239000001282 iso-butane Substances 0.000 description 12
- 229910017052 cobalt Inorganic materials 0.000 description 9
- 239000010941 cobalt Substances 0.000 description 9
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 8
- 229910052750 molybdenum Inorganic materials 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 238000005979 thermal decomposition reaction Methods 0.000 description 7
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910052726 zirconium Inorganic materials 0.000 description 6
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- -1 epoxide compound Chemical class 0.000 description 5
- 150000002432 hydroperoxides Chemical class 0.000 description 5
- 239000011733 molybdenum Substances 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 229910052725 zinc Inorganic materials 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 3
- 229910019589 Cr—Fe Inorganic materials 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000003421 catalytic decomposition reaction Methods 0.000 description 3
- 238000010531 catalytic reduction reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000875 corresponding effect Effects 0.000 description 3
- 239000012969 di-tertiary-butyl peroxide Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 239000002808 molecular sieve Substances 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 150000001451 organic peroxides Chemical class 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 229910052721 tungsten Inorganic materials 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 229910052684 Cerium Inorganic materials 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- WEZJBAOYGIDDLB-UHFFFAOYSA-N cobalt(3+);borate Chemical compound [Co+3].[O-]B([O-])[O-] WEZJBAOYGIDDLB-UHFFFAOYSA-N 0.000 description 2
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-M hydroperoxide group Chemical group [O-]O MHAJPDPJQMAIIY-UHFFFAOYSA-M 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- NIQQIJXGUZVEBB-UHFFFAOYSA-N methanol;propan-2-one Chemical compound OC.CC(C)=O NIQQIJXGUZVEBB-UHFFFAOYSA-N 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 229910052702 rhenium Inorganic materials 0.000 description 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 229940083957 1,2-butanediol Drugs 0.000 description 1
- AKUNSTOMHUXJOZ-UHFFFAOYSA-N 1-hydroperoxybutane Chemical compound CCCCOO AKUNSTOMHUXJOZ-UHFFFAOYSA-N 0.000 description 1
- QMGLMRPHOITLSN-UHFFFAOYSA-N 2,4-dimethyloxolane Chemical compound CC1COC(C)C1 QMGLMRPHOITLSN-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000001668 ameliorated effect Effects 0.000 description 1
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- GVHCUJZTWMCYJM-UHFFFAOYSA-N chromium(3+);trinitrate;nonahydrate Chemical compound O.O.O.O.O.O.O.O.O.[Cr+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O GVHCUJZTWMCYJM-UHFFFAOYSA-N 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- VMKYLARTXWTBPI-UHFFFAOYSA-N copper;dinitrate;hydrate Chemical compound O.[Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O VMKYLARTXWTBPI-UHFFFAOYSA-N 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- SZQUEWJRBJDHSM-UHFFFAOYSA-N iron(3+);trinitrate;nonahydrate Chemical compound O.O.O.O.O.O.O.O.O.[Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O SZQUEWJRBJDHSM-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- AOPCKOPZYFFEDA-UHFFFAOYSA-N nickel(2+);dinitrate;hexahydrate Chemical compound O.O.O.O.O.O.[Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O AOPCKOPZYFFEDA-UHFFFAOYSA-N 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
Definitions
- This invention relates to the catalytic purification of tertiary butyl alcohol prepared by the reaction of propylene with tertiary butyl hydroperoxide. More particularly, this invention relates to a method for the removal of residual contaminating quantities of tertiary butyl hydroperoxide and ditertiary butyl peroxide from a tertiary butyl alcohol feedstock which is prepared by the reaction of propylene with tertiary butyl hydroperoxide and is useful as an octane-enhancing component for motor fuels.
- the peroxide-contaminated feedstock is brought into contact with a catalyst which is either an unsupported nickel, copper, chromia, iron oxide catalyst or a nickel, copper, chromia, iron oxide catalyst supported on silica in order to substantially selectively reduce both the tertiary butyl hydroperoxide and the ditertiary butyl peroxide to tertiary butyl alcohol.
- a catalyst which is either an unsupported nickel, copper, chromia, iron oxide catalyst or a nickel, copper, chromia, iron oxide catalyst supported on silica in order to substantially selectively reduce both the tertiary butyl hydroperoxide and the ditertiary butyl peroxide to tertiary butyl alcohol.
- a process for the manufacture of substituted epoxides from alpha olefins such as propylene is disclosed in Kollar U.S. Pat. No. 3,351,653 which teaches that an organic epoxide compound can be made by reacting an olefinically unsaturated compound with an organic hydroperoxide in the presence of a molybdenum, tungsten, titanium, columbium, tantalum, rhenium, selenium, chromium, zirconium, tellurium or uranium catalyst.
- the hydroperoxide is tertiary butyl hydroperoxide
- propylene oxide and tertiary butyl alcohol are coproducts.
- Pat. No. 3,350,422 teaches a similar process using a soluble vanadium catalyst. Molybdenum is the preferred catalyst. A substantial excess of olefin relative to the hydroperoxide is taught as the normal procedure for the reaction. See also U.S. Pat. No. 3,526,645 which teaches the slow addition of organic hydroperoxide to an excess of olefin as preferred.
- Stein, et al. in U.S. Pat. No. 3,849,451 have improved upon the Kollar process of U.S. Pat. Nos. 3,350,422 and 3,351,635 by requiring a close control of the reaction temperature, between 90°-200° C. and autogeneous pressures, among other parameters.
- Stein et al. also suggests the use of several reaction vessels with a somewhat higher temperature in the last vessel to ensure more complete reaction. The primary benefits are stated to be improved yields and reduced side reactions.
- isobutane can be oxidized with molecular oxygen to form a corresponding tertiary butyl hydroperoxide and that the oxidation reaction can be promoted, for example with an oxidation catalyst (see Johnston U.S. Pat. No. 3,825,605 and Worrell U.S. Pat. No. 4,296,263.
- tertiary butyl alcohol can be prepared either by the direct thermal or catalytic reduction of tertiary butyl hydroperoxide to tertiary butyl alcohol or by the catalytic reaction of propylene with tertiary butyl hydroperoxide to provide propylene oxide and tertiary butyl alcohol.
- tertiary butyl alcohol can be used as an octane-enhancing component when added to a motor fuel, such as gasoline.
- a motor fuel such as gasoline.
- Grane U.S. Pat. No. 3,474,151 to thermally decompose tertiary butyl hydroperoxide and ditertiary butyl peroxide to form tertiary butyl alcohol.
- the thermal decomposition must be conducted with care, as pointed out by Grane, in that tertiary butyl alcohol will start to dehydrate at a temperature of about 450° F. and in that the dehydration becomes rapid at temperatures above about 475° F.
- the product from the thermal decomposition normally contains a minor amount of tertiary butyl hydroperoxide and ditertiary butyl peroxide which have an adverse effect upon the quality of motor fuels and must be substantially completely removed if the tertiary butyl alcohol is to be fully effective.
- Grane proposes to accomplish this thermally by heating tertiary butyl alcohol containing small quantities of such peroxides at a temperature of 375°-475° F. for a period of 1 to 10 minutes.
- the product of this thermal decomposition step still contained residual tertiary butyl hydroperoxide, most of which was thereafter removed by a final thermal treatment of the contaminated tertiary butyl hydroperoxide in the manner taught by Grane U.S. Pat. No. 3,474,151.
- the tertiary butyl hydroperoxide residual content will normally be about 0.1 to about 1 wt. %, based on the tertiary butyl alcohol, while the residual ditertiary butyl peroxide content, if any, will only be about 0.1 to 0.5 wt. %.
- Mabuchi et al. U.S. Pat. No. 4,112,004 discloses a process for preparing monohydric or polyhydric alcohols from organic peroxides in the presence of a nickel catalyst by continuously feeding a solution of the organic peroxide (e.g., butadiene peroxide) and a suspension of the nickel catalyst to a reactor in a controlled ratio and continuously withdrawing reaction mixture at a rate adequate to maintain a constant weight and composition of the reaction mixture in the reactor.
- a nickel catalyst by continuously feeding a solution of the organic peroxide (e.g., butadiene peroxide) and a suspension of the nickel catalyst to a reactor in a controlled ratio and continuously withdrawing reaction mixture at a rate adequate to maintain a constant weight and composition of the reaction mixture in the reactor.
- Godfrey U.S. Pat. No. 3,037,025 discloses the preparation of N-alkyl substituted piperazines using catalyst compositions consisting of the metals and oxides of copper, nickel and cobalt (including mixtures thereof) which may also be promoted by the inclusion of a normally non-reducible metal oxide such as chromium, aluminum, iron, calcium, magnesium, manganese and the rare earths.
- Preferred catalyst compositions are indicated as containing from about 44 to about 74 wt. % of nickel, about 5 to about 55 wt. % of copper and about 1 to about 5 wt. % of chromia.
- Moss U.S. Pat. No. 3,151,112 discloses catalyst compositions useful for the preparation of morpholines including one or more metals from the group including copper, nickel, cobalt, chromium, molybdenum, manganese, platinum, palladium and rhodium, which may also be promoted with normally nonreducible oxides such as chromium oxide, molybdenum oxide and manganese oxide.
- Representative catalyst compositions include those containing from about 60 to about 85 wt. % of nickel, about 14 to about 37 wt. % of copper and about 1 to about 5 wt. % of chromia.
- Nickel, copper, chromia catalysts are also disclosed in Moss U.S. Pat. No. 3,151,115 and Moss U.S. Pat. No. 3,152,998.
- Winderl et al. U.S. Pat. No. 3,270,059 teaches the use of catalysts containing a metal of groups I-B and VIII of the Periodic System. Examples of suitable catalysts are stated to be copper, silver, iron, nickel, and particularly, cobalt.
- Boettger et al. U.S. Pat. No. 4,014,933 discloses catalysts containing cobalt and nickel promoted with copper such as those containing from about 70 to about 95 wt. % of a mixture of cobalt and nickel and from about 5 to about 30 wt. % of copper.
- Habermann U.S. Pat. No. 4,152,353 discloses catalyst compositions comprising nickel, copper and a third component which may be iron, zinc, zirconium or a mixture thereof such as catalysts containing from about 20 to about 49 wt. % of nickel, about 36 to about 79 wt. % of copper and about 1 to about 15 wt. % of iron, zinc, zirconium or a mixture thereof. Similar catalyst compositions are mentioned in Habermann U.S. Pat. No. 4,153,581.
- European patent application No. 0017651 filed Oct. 20, 1980 contains a disclosure of catalyst compositions related to those disclosed by Habermann, such catalyst compositions being composed of nickel or cobalt, copper and iron, and zinc or zirconium such as compositions containing 20 to 90% cobalt, 3 to 72% copper and 1 to 16% of iron, zinc or zirconium and catalyst compositions containing 20 to 49% nickel, 36 to 79% copper and 1 to 16% of iron, zinc or zirconium.
- German Offen. No. 2,721,033 discloses a catalyst composition containing 35% nickel, about 87.5% iron and a minor amount of chromia.
- the feedstocks of the present invention comprise tertiary butyl alcohol contaminated with tertiary butyl hydroperoxide and ditertiary butyl peroxide.
- the reaction product When isobutane is treated to form tertiary butyl hydroperoxide, the reaction product will normally contain some tertiary butyl alcohol and other oxygenated by-products such as ditertiary butyl peroxide, acetone, etc., as well as unreacted isobutane. After the unreacted isobutane is flashed, a fraction composed mostly of tertiary butyl alcohol may be recovered as a distillate fraction in order to further concentrate the desired tertiary butyl hydroperoxide reaction product.
- tertiary butyl alcohol distillate which will normally be contaminated with tertiary butyl hydroperoxide, ditertiary butyl peroxide, etc., may be used as a feedstock for the process of the present invention.
- Tertiary butyl alcohol is suitably reacted with propylene by a process of the type disclosed in Kollar U.S. Pat. No. 3,351,635 to provide an initial reaction product composed mostly of unreacted propylene, propylene oxide and tertiary butyl alcohol.
- residual qua ntities of tertiary butyl hydroperoxide and ditertiary butyl peroxide and other oxygenated impurities are normally present and remain dissolved in the tertiary butyl alcohol recovered from the reaction mixture.
- This tertiary butyl alcohol product can also be used as a feedstock for the process of the present invention.
- Tertiary butyl hydroperoxide can decompose thermally and/or catalytically to form acetone.
- Tertiary butyl alcohol can be decomposed to form water and isobutylene. Accordingly, the tertiary butyl alcohol, as initially recovered is not entirely satisfactory for use as an octane-enhancing component for motor fuels, such as gasoline. Thus, tertiary butyl alcohol will normally be considered unsatisfactory for motor fuel use if it contains more than about 3 wt. % of acetone, more than about 1 wt.
- the tertiary butyl alcohol will contain about 1 wt. % or less of acetone, 0.5 wt. % or less of isobutylene and 10 ppm or less of ditertiary butyl peroxide and 100 ppm or less of tertiary butyl hydroperoxide.
- motor-fuel grade tertiary butyl alcohol which is contaminated with residual amounts of ditertiary butyl peroxide and tertiary butyl hydroperoxide can be effectively catalytically treated with an unsupported catalyst compound of nickel, copper, chromia, iron oxide or a nickel, copper, chromia, iron oxide catalyst supported on silica under mild catalytic conditions including a temperature of about 80° to 220° C. at a pressure sufficient to maintain a liquid phase reaction mixture (normally, about 200 to 800 psig., depending on reaction temperature. Higher pressures of up to about 2000 psig. can be used, if desired, but there is no particular advantage in using the higher pressures.
- This treatment will substantially selectively convert the peroxide contaminants to tertiary butyl alcohol and thereby provide a treated product substantially free of contaminating quantites of tertiary butyl hydroperoxide and ditertiary butyl peroxide.
- the formation of unwanted oxygenated derivatives of the peroxide contaminates, including acetone, methanol and isobutylene is substantially avoided.
- the starting materials for the process of the present invention include a motor-fuel grade tertiary butyl alcohol feedstock obtained in the manner described above by the reaction of propylene with tertiary butyl hydroperoxide to form propylene oxide and tertiary butyl alcohol by the oxidation of isobutane to form tertiary butyl hydroperoxide, etc.
- the motor-fuel grade tertiary butyl alcohol feedstock obtained by the reaction of propylene with tertiary butyl hydroperoxide to form propylene oxide and tertiary butyl alcohol will contain contaminating quantities of teritary butyl hydroperoxide, ditertiary butyl peroxide, and acetone, and may also contain contaminating quantities of methanol and isobutylene.
- the normal levels of contamination of such materials are such that the tertiary butyl alcohol will normally contain, prior to treatment, from about 0.1 to about 5 wt. % of tertiary butyl hydroperoxide and from about 0.1 to about 5 wt. % of ditertiary butyl peroxide. Minor quantities of other contaminants may also be present.
- the feedstock to be used for the practice of the present invention is an impure motor grade tertiary butyl alcohol containing from about 0.1 to about 5 wt. % of tertiary butyl hydroperoxide and from about 0.1 to about 5 wt. % of ditertiary butyl peroxide.
- the catalyst compositions of the present invention consist essentially of the oxides of and/or metallic nickel, copper, chromia and iron in the proportions (on an oxygen-free basis) of about 1 to about 20 wt. % of iron, about 1 to about 6 wt. % of chromia and with the balance being nickel and copper in the weight ratio of about 2 to 3 parts of nickel per part of copper.
- the catalyst compositions of the present invention may consist essentially of about 30 to about 60 wt. % of nickel, about 5 to about 40 wt. % of copper, about 0.5 to about 10 wt. % of chromia and about 1 to about 30 wt. % of iron, with the nickel and copper being proportioned as indicated above.
- the catalyst compositions of the present invention will contain about 1 to about 20 wt. % of iron and about 1 to about 5 wt. % of chromia, with the nickel and copper being proportioned as indicated above.
- the catalyst compositions of the present invention may be composed of one or more of the oxides of nickel, copper, chromium and iron in the proportions (calculated on an oxygen-free basis) given above.
- an oxide catalyst When an oxide catalyst is prepared, it will tend to be reduced to the metallic form during use.
- the catalyst may also be supported on a suitable silica support such as Kieselguhr.
- the catalyst compositions of the present invention may be utilized in powdered form in conducting batch reactions, their utility is enhanced when they are used in pelleted form for catalyzing the reaction in a continuous process.
- a catalyst is used in pelleted form for a continuous reaction, it is necessary that the pellets have good physical and chemical properties so that they will not disintegrate or break during the course of the continuous peroxide reduction.
- the catalyst compositions of the present invention have such properties.
- a tertiary butyl alcohol feedstock as above described, is brought into contact with a catalyst of the present invention under reaction conditions correlated to substantially selectively catalytically convert both the tertiary butyl hydroperoxide and ditertiary butyl peroxide contaminants in the tertiary butyl alcohol feedstock to tertiary butyl alcohol with not more than a minor increase in the level of contamination of the acetone, methanol and isobutylene also normally present in the tertiary butyl alcohol as contaminants.
- the reaction may be conducted batchwise in an autoclave using powdered catalyst or may be conducted on a continuous basis by passing the tertiary butyl alcohol through a reactor containing a bed of a catalyst of the present invention under reaction conditions including a temperature within the range of about 80° to about 280° C. and, more preferably, from about 110 to about 180° C.
- the reaction is preferably conducted at 200 to 800 psig., although higher pressures of up to about 2000 psig. may be used if desired.
- contact time may suitably be from about 0.5 to about 4 hours.
- the tertiary butyl alcohol should be passed over the bed of catalyst at a liquid hourly space velocity of about 0.25 to about 5.
- reaction product after being degassed, is suitable for use as an octane-enhancing component of motor fuel, such as gasoline.
- the effluent from the reactor may be passed through a phase separation zone in order to permit gaseous reaction components including hydrogen and isobutane to volatilize from the product to thereby provide the desired reaction product.
- any specific catalyst of the present invention can be determined by one of ordinary skill in the art with comparative ease.
- the tertiary butyl alcohol feedstock should be analyzed prior to catalytic treatment to determine the level of contamination by tertiary butyl hydroperoxide, ditertiary butyl peroxide, acetone, methanol and isobutylene. If there is an insufficient reduction of the hydroperoxides such that a significant amount (e.g., more than about 0.1 wt.
- reaction conditions are not sufficiently severe, and should be increased such as, for example, by increasing reaction temperature or contact time in order to obtain the desired reduction of the tertiary butyl hydroperoxide.
- reaction conditions are too severe for the particular catalyst and the reaction conditions should be ameliorated (e.g., by reducing contact time or temperature).
- Graphite (1%) was added to a portion of the reduced and stabilized catalyst and this material was formed into 1/8 in. diameter ⁇ 1/8 in. pellets.
- the catalyst was found to contain 51.2 wt. % Ni, 17.4 wt. % Cu, 2.9 wt. % Cr and 8.2 wt. % Fe.
- Ni-Cu-Cr-Fe catalyst essentially the same amounts of materials and procedures were used as described in 5676-72 (above) in the preparation of this Ni-Cu-Cr-Fe catalyst, except that only 75% of the sodium carbonate solution was added and, consequently, not all of the nickel precipitated.
- the resultant catalyst contained 45.3 wt. % Ni, 26.7 wt. % Cu, 3.4 wt. % Cr and 9.9 wt. % Fe. A portion of the catalyst was formed into 1/8 in. diameter ⁇ 1/8 in. pellets.
- run 6064-60-1 the feedstock was heated in the reactor at a temperature of about 160° C. and a pressure of about 520 psig., being passed to the reactor at the rate of about 0.9 lbs/hr.
- Table II there was a significant reduction in the level of tertiary butyl hydroperoxide contamination, but only a minor decrease in the level of contamination due to ditertiary butyl peroxide. Note also there was a significant increase in the level of contamination due to the formation of acetone.
- the catalysts included a supported cobalt catalyst (catalyst AA), a manganese catalyst (catalyst BB), a tungsten catalyst (catalyst CC), a vanadia catalyst (catalyst DD), a molybdena catalyst (catalyst EE), two copper chromite catalysts (catalysts FF and KK), a rhodium on alumina catalyst (catalyst HH), a catalyst containing three metallic oxides (catalyst II), a promoted iron oxide catalyst (catalyst JJ), a nickel, copper, chromia catalyst (catalyst OO), a promoted iron oxide catalyst (catalyst RR), a promoted chromia catalyst (catalyst SS) and a molecular sieve catalyst (catalyst TT).
- catalysts GG and LL of the present invention were also evaluated.
- Triplicate run 6089-36 and triplicate run 6089-42 are directed to the evaluation of a nickel, copper, chromia catalyst supported on iron (catalyst LL). With this catalyst, good reductions in the level of contamination by ditertiary butyl peroxide were obtained at temperatures of 140°-160° and feed rates of about 0.2 lbs/hr (runs 6089-35-1, 6089-35-2 and 6089-35-3).
- Runs 6089-36-1, 6089-36-2 and 6089-36-3 were conducted at feed rates of about 1 lb/hr and again, an acceptable level of reduction of contamination by ditertiary butyl peroxide was obtained, although not so good as the previous run, but much better results insofar as contamination by acetone, methanol and isobutylene are concerned. Good results were also obtained in quadruplicate runs 6089-42 using higher temperatures ranging from 170° to 200° C.
- a reference catalyst, nickel, copper, chromia (catalyst XX) was evaluated in runs 6129-39, 6129-40 and 6129-41. Higher levels of ditertiary butyl peroxide contamination in the product, as well as higher levels of isobutylene contamination were noted, as compared with the other catalyst.
- a molybdenum promoted nickel, copper, chromia catalyst was also evaluated (catalyst YY) in runs 6129-74, 6129-75 and 6129-76. Although very low levels of ditertiary butyl peroxide contamination were obtained, the levels of isobutylene contamination were excessive.
- Catalyst VV contained very low levels of Ni, Cu, Cr, Fe and was therefore not as active. The low levels of metals in this catalyst are outside our preferred catalyst composition ranges.
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Abstract
Description
TABLE I
______________________________________
Catalysts for Peroxide Decomposition
Code Catalyst Description
______________________________________
AA 25% Cobalt on a proprietary silica-alumina
support, 1/8" extrusions
BB Unsupported manganese catalyst, 1/8" tablets
CC 19% W, 6% Ni on silica support, 3/16" extrusions
DD 10% V.sub.2 O.sub.5 on a silica-alumina support, 3/16"
extrusions
EE Unsupported 55% Mo and 11% Fe, 1/8" tablets
(As moles of metals and metal oxides)
FF Copper Chromite (79% CuO, 17% Cr.sub.2 O.sub.3), 1/8" tablets
GG Ni 30.7%, Cu 12.6%, Fe 3.3%, Cr 0.64% (as moles of
metals and metal oxides)
HH 0.5% Rh on Alumina, 1/8" pellets
II 45% Ni, 5% Co, 4.5% Cu on 50% Silica, 1/8" tablets
JJ 58% Fe.sub.2 O.sub.3, 23% K.sub.2 CO.sub.3, 5% Ce.sub.2 O.sub.3,
2.5% MoO.sub.3,
1/8" extrusions
KK 39% CuO, 8.5% Cr.sub.2 O.sub.3 on 50% SiO.sub.2, 1/8" tablets
LL 49.1% Ni, 13.9% Cu, 1.1% Cr, 17.4T Fe
MM 5676-72, See catalyst preparation
NN 5676-66, See catalyst preparation
OO 50.0% Ni, 15.0% Cu, 0.6% Cr
RR 58% Fe.sub.2 O.sub.3, 33% K.sub.2 CO.sub.3, 5% Ce.sub.2 O.sub.3,
2.5% MoO.sub.3,
1/16" extrusions
SS 89% Fe.sub.2 O.sub.3, 9% Cr.sub.2 O.sub.3, irregular
TT 13 X Molecular sieves, 1/16" pellets
VV 0.44% Fe, 0.10% Cr, 0.21% Cu, 1% Ni on 97% SiO.sub.2,
1/8" tablets
XX 77% Ni, 12% Cu, 2% Cr, 1/8" extrusions
YY 56.5% Ni, 20.3% Cu, 3.2% Cr, 8.5% Mo
______________________________________
TABLE II
__________________________________________________________________________
Catalytic Decomposition of Peroxides in tert-Butyl Alcohol
N.B. Cat.
Temp.
Feed
Pressure
H.sub.2 O
TBHP Products by GC Analysis, Wt. %
Number
Code
(°C.)
#/Hr
(psig)
(wt. %)
(ppm)
DTBP
Acetone
MeOH
IB=
__________________________________________________________________________
5787-76-1
(Feed) 1.7 1555 0.117
0.002
0.003
˜0
6064-60-1
None
160 0.90
520 1.8 227 0.095
0.033
0.002
˜0
6064-77-1
AA 80 1.04
500 1.7 113 0.118
0.010
˜0
˜0
2 120 0.99
500 1.7 6.13 0.118
0.016
0.001
0.00077
3 160 1.00
500 1.7 4.76 0.100
0.033
0.002
0.010
6064-82-1
BB 80 1.02
500 1.77 113 0.116
0.010
˜0
˜0
2 120 1.00
500 1.74 10.99
0.116
0.017
˜0
˜0
3 160 1.00
500 1.72 3.71 0.102
0.036
0.001
0.00097
6064-84-1
CC 120 0.99
500 1.74 238 0.107
0.002
˜0
0.003
2 80 1.02
500 1.72 162 0.116
0.00097
˜0
˜0
3 160 1.00
500 1.90 201 0.101
0.020
0.001
0.331
6064-87-1
DD 80 0.99
500 2.7 692 0.117
0.004
0.002
0.284
2 120 0.96
500 3.9 178 0.121
0.019
0.003
2.330
3 160 0.95
500 8.8 12.73
0.111
0.044
0.002
3.853
6064-90-1
EE 80 0.91
500 1.7 563 0.119
0.003
0.002
0.029
2 120 1.00
500 2.2 488 0.119
0.003
0.002
1.021
3 160 1.02
500 6.6 136 0.116
0.026
0.001
4.588
6064-92-1
FF 80 1.02
500 1.7 282 0.116
0.004
0.002
0.003
2 120 0.99
500 1.7 184 0.115
0.012
0.004
0.001
3 160 1.00
500 1.8 15.8 0.102
0.051
0.006
0.011
6064-93-1
GG 80 1.02
500 1.7 195 0.102
0.007
0.004
0.005
2 120 1.00
500 1.7 12.5 0.089
0.009
0.004
0.002
3 160 1.00
500 1.7 8.48 0.032
0.051
0.004
0.038
6064-96-1
HH 80 0.95
500 1.73 57.7 0.107
0.011
0.003
˜0
2 120 1.00
500 1.71 21.6 0.105
0.015
0.003
˜0
3 160 1.00
500 1.71 11.7 0.092
0.028
0.003
0.001
6064-98-1
II 80 1.04
500 1.70 103.6
0.119
0.014
0.003
˜ 0
2 120 1.01
500 1.70 23.9 0.107
0.018
0.003
0.014
3 160 1.00
500 1.90 12.4 0.087
0.028
0.004
0.368
6064-99-1
JJ 80 1.05
500 1.63 219 0.105
0.003
0.003
0.002
2 120 1.00
500 1.69 203 0.106
0.005
0.003
˜0
3 160 0.92
500 1.71 223 0.094
0.024
0.003
0.001
6064-100-1
KK 80 1.01
500 1.74 203 0.105
0.003
0.003
˜0
2 120 1.00
500 1.72 212 0.106
0.009
0.004
0.003
3 160 1.03
500 1.73 14.9 0.082
0.061
0.008
0.033
6089-6-1
GG 160 1.04
500 1.71 22.1 0.026
0.044
0.004
0.045
2 200 1.02
500 2.03 21.6 0.008
0.266
˜0
0.575
3 240 1.02
500 4.68 10.6 0.004
0.302
0.001
3.366
6089-7-1
GG 160 0.21
500 1.97 25.5 0.012
0.165
0.002
0.159
2 200 0.25
500 2.23 22.1 0.003
0.246
˜0
1.909
3 240 0.28
500 -- 14.0 0.003
0.511
˜0
1.934
6089-12-1
GG 140 0.23
500 2.15 20.7 0.014
0.097
0.003
0.321
2 180 0.22
500 4.08 22.5 0.006
0.240
˜0
3.319
__________________________________________________________________________
TABLE III
__________________________________________________________________________
Catalytic Decomposition of Peroxides in tert-Butyl Alcohol
N.B. Cat.
Temp.
Feed
Press.
H.sub.2 O
Products by GC Analysis, Wt. %
Number
Code
(°C.)
#/Hr
(psig)
wt. %
DTBP
Acetone
MeOH
IB═
__________________________________________________________________________
5787-80-1
(Feed) 0.11
0.839
0.002
0.003
˜0
6089-19-1
GG 140 0.94
500 0.22
0.409
0.111
0.001
0.185
2 160 0.98
500 0.38
0.196
0.176
0.003
0.643
3 180 1.00
500 0.89
0.045
0.265
0.002
1.498
6089-20-1
GG 140 0.19
500 0.47
0.010
0.345
0.002
0.713
2 160 0.20
500 1.02
0.006
0.345
0.002
2.313
3 180 0.21
500 2.51
0.008
0.357
0.004
5.100
6089-35-1
LL 140 0.21
500 0.08
0.118
0.076
0.006
0.009
2 150 0.22
500 0.08
0.022
0.122
0.005
0.013
3 160 0.21
500 0.13
0.017
0.211
0.006
0.014
6089-36-1
LL 140 0.95
500 0.09
0.406
0.022
0.003
0.004
2 150 0.99
500 0.06
0.316
0.035
0.003
0.004
3 160 1.00
500 0.15
0.190
0.067
0.003
0.006
6089-42-1
LL 170 1.03
500 0.10
0.195
0.165
0.005
0.005
2 180 1.04
500 0.10
0.075
0.241
0.005
0.012
3 190 1.02
500 0.13
0.017
0.321
0.004
0.042
4 200 0.98
500 0.21
0.018
0.399
0.002
0.077
6089-39-1
MM 140 0.26
500 0.27
0.333
0.074
0.003
0.003
2 150 0.20
500 0.47
0.093
0.259
0.004
0.005
3 160 0.20
500 0.35
0.019
0.408
0.003
0.009
6089-40-1
MM 140 1.02
500 0.11
0.680
0.027
˜0
0.001
2 150 0.98
500 0.13
0.618
0.050
˜0
0.002
3 160 1.00
500 0.10
0.522
0.090
˜0
0.003
6787-80-2
(Feed) 0.12
0.835
0.002
0.002
0.001
6089-49-1
MM 170 0.96
500 -- 0.362
0.154
0.001
0.004
2 180 0.97
500 0.12
0.221
0.235
˜0
0.005
3 190 0.96
500 0.14
0.094
0.322
0.001
0.004
4 200 0.97
500 0.18
0.027
0.448
˜0
0.014
6089-51-1
NN 130 0.20
500 0.29
0.356
0.064
˜0
0.002
2 140 0.21
500 0.07
0.062
0.059
˜0
0.002
3 150 0.19
500 0.04
0.053
0.094
˜0
0.005
4 160 0.23
500 0.07
0.003
0.100
0.001
0.006
6089-52-1
130 0.98
500 0.06
0.613
0.017
˜0
0.001
2 140 0.97
500 0.09
0.532
0.029
˜0
0.001
3 150 1.04
500 0.06
0.433
0.045
˜0
0.001
4 160 0.99
500 0.04
0.304
0.075
0.001
0.002
6089-53-1
170 1.07
500 0.06
0.218
0.124
0.001
0.004
2 180 1.04
500 0.12
0.102
0.210
˜0
0.007
3 190 1.03
500 0.04
0.030
0.273
0.002
0.011
4 200 1.00
500 0.06
0.011
0.293
0.001
0.017
6089-59-1
OO 130 0.20
500 0.07
0.596
0.051
0.002
0.045
2 140 0.21
500 0.12
0.507
0.088
0.004
0.070
3 150 0.23
500 0.14
0.359
0.168
0.006
0.115
4 160 0.22
500 0.18
0.101
0.202
0.006
0.162
6089-60-1
130 1.08
500 0.01
0.783
0.011
˜0
0.012
2 140 1.10
500 0.01
0.727
0.023
0.001
0.027
3 150 1.08
500 0.17
0.599
0.074
0.002
0.072
4 160 1.08
500 0.16
0.564
0.096
0.003
0.078
6089-61-1
170 1.02
500 0.03
0.457
0.162
0.004
0.089
2 180 0.98
500 0.17
0.292
0.269
0.005
0.156
3 190 1.06
500 0.18
0.164
0.351
0.006
0.167
4 200 1.03
500 0.24
0.025
0.450
0.006
0.319
5787-100-2
(Feed) 0.05
0.812
0.002
˜0
0.002
6089-73-1
RR 130 0.22
500 0.14
0.803
0.035
˜0
0.0008
2 140 0.19
500 0.10
0.716
0.121
0.0006
0.001
3 150 0.18
500 0.21
0.570
0.241
˜0
0.001
4 160 0.20
500 0.11
0.326
0.450
0.0004
0.0008
6089-74-1
130 1.00
500 0.08
0.858
0.009
0.0008
0.0008
2 140 1.00
500 0.11
0.843
0.020
0.001
0.0009
3 150 0.97
500 0.11
0.813
0.045
0.0009
0.001
4 160 0.98
500 0.10
0.731
0.116
0.0008
0.002
5787-100-4
(Feed) 0.07
0.896
0.002
˜0
0.002
6089-75-1
170 0.98
500 0.09
0.591
0.233
0.0007
0.002
2 180 1.02
500 0.06
0.404
0.454
0.001
0.002
3 190 0.96
500 0.16
0.148
0.681
0.0008
0.002
4 200 0.96
500 0.06
0.021
0.658
0.0006
0.0008
6089-76-1
SS 130 0.25
500 0.14
1.313
0.052
0.001
0.007
2 140 0.23
500 0.11
0.627
0.068
0.0005
0.013
3 150 0.19
500 0.09
0.622
0.184
0.0009
0.017
4 160 0.22
500 0.10
0.305
0.326
0.001
0.022
6089-77-1
130 0.95
500 0.12
0.995
0.022
0.0005
0.002
2 140 0.99
500 0.09
0.980
0.028
0.0006
0.003
3 150 0.98
500 0.08
0.929
0.052
0.001
0.005
4 160 0.97
500 0.08
0.841
0.121
0.0007
0.010
6089-78-1
170 1.00
500 0.07
0.675
0.231
0.0008
0.015
2 180 1.02
500 0.11
0.443
0.384
0.001
0.024
3 190 0.99
500 0.11
0.158
0.559
˜0
0.041
4 200 1.00
500 0.17
0.018
0.643
0.002
0.111
6123-1-1
(Feed) 0.06
0.843
0.002
˜0
0.001
6129-39-1
XX 130 0.22
500 0.17
0.416
0.072
0.003
0.011
2 140 0.18
500 0.14
0.189
0.196
0.002
0.014
3 150 0.22
500 0.19
0.137
0.277
0.003
0.066
4 160 0.17
500 0.32
0.015
0.346
0.002
0.214
6129-40-1
130 0.97
500 0.09
0.729
0.058
˜0
0.007
2 140 1.00
500 0.09
0.731
0.071
˜0
0.017
3 150 0.98
500 0.11
0.692
0.089
˜0
0.033
4 160 1.00
500 0.15
0.587
0.152
˜0
0.071
6129-41-1
170 0.98
500 0.28
0.732
0.382
˜0
0.104
2 180 0.96
500 0.31
0.250
0.358
0.004
0.178
3 190 1.02
500 0.32
0.046
0.332
˜0
0.266
4 200 1.03
500 0.39
0.004
0.262
˜0
0.234
6129-74-1
YY 130 0.20
500 0.12
0.003
0.064
0.006
0.111
2 140 0.19
500 0.19
0.002
0.072
0.005
0.289
3 150 0.19
500 0.35
˜0
0.072
0.007
0.290
4 160 0.20
500 0.47
˜0
0.093
0.007
0.865
6129-75-1
130 1.00
500 0.15
0.564
0.022
0.002
0.032
2 140 1.00
500 0.12
0.313
0.051
0.005
0.069
3 150 0.93
500 0.30
0.015
0.219
˜0
0.184
4 160 0.95
500 0.06
0.053
0.094
0.009
0.194
6129-76-1
170 1.16
500 0.32
0.033
0.155
˜0
0.432
2 180 1.05
500 0.20
0.125
0.119
0.010
0.185
3 190 1.05
500 0.45
0.009
0.182
0.001
0.729
4 200 1.01
500 0.73
0.003
0.226
0.011
1.239
6123-2-2
(Feed) 0.05
0.841
˜0
˜0
0.003
6129-7-1
TT 130 0.2
500 0.71
0.756
0.022
˜0
0.251
2 140 0.2
500 0.39
0.710
0.050
˜0
0.677
3 150 0.2
500 0.66
0.586
0.116
˜0
1.234
4 160 0.2
500 1.30
0.335
0.258
˜0
2.154
6129-8-1 130 1.0
500 0.10
0.784
˜0
˜0
0.167
2 140 1.0
500 0.20
0.776
0.013
˜0
0.368
3 150 1.0
500 0.30
0.754
0.028
˜0
0.699
4 160 1.0
500 0.60
0.687
0.064
˜0
1.359
6129-9-1 170 1.0
500 1.00
0.570
0.135
˜0
1.501
2 180 1.0
500 1.40
0.386
0.241
˜0
2.017
3 190 1.0
500 2.00
0.150
0.375
˜0
2.615
4 200 1.0
500 2.60
0.035
0.469
˜0
4.144
6129-35-1
VV 130 0.2
500 0.07
0.667
0.053
0.002
0.002
2 140 0.2
500 0.07
0.516
0.124
0.004
0.004
3 150 0.2
500 0.08
0.367
0.224
˜0
0.007
4 160 0.2
500 0.07
0.144
0.371
˜0
0.009
6129-36-1
130 1.0
500 0.06
0.771
0.011
˜0
0.001
2 140 1.0
500 0.05
0.742
0.025
0.0004
0.002
3 150 1.0
500 0.05
0.688
0.058
0.001
0.003
4 160 1.0
500 0.06
0.590
0.124
0.002
0.006
6129-37-1
170 1.0
500 0.04
0.436
0.226
0.004
0.008
2 180 1.0
500 0.06
0.218
0.385
0.005
0.009
3 190 1.0
500 0.07
0.055
0.497
0.005
0.009
4 200 1.0
500 0.07
0.011
0.540
0.005
0.011
6123-1-2
(Feed) 0.03
0.843
0.002
˜0
0.001
6129-44-1
LL 140 0.5
500 0.03
0.377
0.047
˜0
0.005
2 160 0.5
500 0.17
0.115
0.119
˜0
0.008
3 200 0.5
500 0.09
0.005
0.247
˜0
0.092
6123-4-1
(Feed) 0.04
0.434
0.011
˜0
0.009
6129-45-1
140 0.2
500 0.10
0.012
0.104
˜0
0.002
2 160 0.2
500 0.09
0.008
0.041
˜0
˜0
3 180 0.2
500 0.19
0.006
0.251
˜0
0.084
4 200 0.2
500 0.50
0.007
0.268
˜0
0.417
6129-46-1
140 0.5
500 0.05
0.170
0.065
˜0
0.007
2 160 0.5
500 0.09
0.015
0.161
˜0
0.012
3 180 0.5
500 0.16
0.011
0.248
˜0
0.026
4 200 0.5
500 0.25
0.006
0.256
˜0
0.159
6129-47-1
140 1.0
500 0.07
0.218
0.066
˜0
0.004
2 160 1.0
500 0.06
0.125
0.108
˜0
0.005
3 180 1.0
500 0.07
0.035
0.172
˜0
0.007
4 200 1.0
500 0.10
0.008
0.217
˜0
0.047
__________________________________________________________________________
Claims (19)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/879,660 US4704482A (en) | 1986-06-27 | 1986-06-27 | Catalytic purification of tertiary butyl alcohol |
| DE8787305118T DE3766429D1 (en) | 1986-06-27 | 1987-06-10 | CATALYTIC CLEANING OF TERTIA BUTANOL. |
| EP87305118A EP0251526B1 (en) | 1986-06-27 | 1987-06-10 | Catalytic purification of tertiary butyl alcohol |
| JP62156717A JP2504993B2 (en) | 1986-06-27 | 1987-06-25 | Method for catalytic purification of tert-butyl alcohol |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/879,660 US4704482A (en) | 1986-06-27 | 1986-06-27 | Catalytic purification of tertiary butyl alcohol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4704482A true US4704482A (en) | 1987-11-03 |
Family
ID=25374613
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/879,660 Expired - Lifetime US4704482A (en) | 1986-06-27 | 1986-06-27 | Catalytic purification of tertiary butyl alcohol |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4704482A (en) |
| EP (1) | EP0251526B1 (en) |
| JP (1) | JP2504993B2 (en) |
| DE (1) | DE3766429D1 (en) |
Cited By (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5124492A (en) * | 1991-02-12 | 1992-06-23 | Uop | Process for decomposing peroxide impurities in a tertiary butyl alcohol feedstock using an iron (II) compound |
| US5196603A (en) * | 1991-02-12 | 1993-03-23 | Uop | Process for decomposing peroxide impurities in a teritary butyl alcohol feedstock using an iron (II) compound |
| EP0541312A1 (en) * | 1991-11-04 | 1993-05-12 | Texaco Chemical Company | Catalytic decomposition of impurities in methyl tertiary butyl ether |
| EP0555592A1 (en) * | 1992-02-10 | 1993-08-18 | Texaco Chemical Inc. | Catalytic decomposition of impurities in methyl tertiary butyl ether |
| US5243101A (en) * | 1992-06-12 | 1993-09-07 | Texaco Chemical Company | Removal of peroxide contaminants from tertiary butyl alcohol |
| US5254759A (en) * | 1992-06-12 | 1993-10-19 | Texaco Chemical Company | Catalytic removal of peroxide contaminants from tertiary butyl alcohol |
| EP0581530A1 (en) * | 1992-07-28 | 1994-02-02 | Texaco Chemical Inc. | Catalytic removal of peroxide contaminants from a methanol-tertiary butyl alcohol recycle stream |
| EP0653401A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported palladium, catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653407A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Conjoint production of ditertiary butyl peroxide and tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653403A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of titania or zirconia in the preparation of tertiary butyl alcohol from tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653402A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported lead oxide catalyst in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653404A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported chromium catalyst in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653406A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported rhodium catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653405A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported palladium/platinum catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| US5436376A (en) * | 1994-08-11 | 1995-07-25 | Texaco Chemical Inc. | Production of tertiary butyl alcohol |
| EP0710640A1 (en) | 1994-11-01 | 1996-05-08 | Texaco Development Corporation | Recovery and purification of tertiary butyl alcohol |
| US5583266A (en) * | 1994-05-02 | 1996-12-10 | Texaco Inc. | Integrated process for the production of isopropyl alcohol and diisopropyl ethers |
| US5741952A (en) * | 1992-02-10 | 1998-04-21 | Huntsman Specialty Chemicals Corporation | Catalytic decomposition of peroxides to purify a methyl tertiary butyl ether recycle stream |
| WO1999024384A1 (en) * | 1997-11-10 | 1999-05-20 | Huntsman Specialty Chemicals Corporation | Methods for decomposing esters and purifying alcohols |
| US6037516A (en) * | 1997-11-20 | 2000-03-14 | Huntsman Ici Chemicals Llc | Method for removal of oxygenate impurities from organic chemical streams |
| US6133484A (en) * | 1996-10-07 | 2000-10-17 | Huntsman Ici Chemical Llc | Methods for decomposing esters and purifying alcohols |
| US6518474B1 (en) | 1999-10-29 | 2003-02-11 | Huntsman International Llc | Process for producing isobutylene from tertiary butyl alcohol |
| WO2003048092A1 (en) | 2001-12-03 | 2003-06-12 | Arco Chemical Technology, L.P. | Purification of tertiary butyl alcohol |
| US6613108B1 (en) * | 1998-10-16 | 2003-09-02 | Fortum Oil & Gas Oy | Process for producing a fuel component |
| US20090269834A1 (en) * | 2008-04-25 | 2009-10-29 | Quinn Thomas J | Micro refinery system for ethanol production |
| CN111097510A (en) * | 2018-10-29 | 2020-05-05 | 中国石油化工股份有限公司 | TBA refined catalyst, preparation method and application thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4873380A (en) * | 1987-01-20 | 1989-10-10 | Texaco Inc. | Catalyst for removing peroxide contaminants from tertiary butyl alcohol |
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| US2854487A (en) * | 1955-04-12 | 1958-09-30 | Distillers Co Yeast Ltd | Process for the manufacture of carbinols |
| US2993072A (en) * | 1956-06-15 | 1961-07-18 | Montedison Spa | Process for obtaining carboxylic acids from organic peroxides and carbon monoxide |
| US3360584A (en) * | 1965-05-25 | 1967-12-26 | Halcon International Inc | Process for the co-production of isoprene and oxygenated compounds from isopentane hydroperoxide |
| US3624165A (en) * | 1969-04-25 | 1971-11-30 | Monsanto Co | Purification process |
| US3914295A (en) * | 1972-12-18 | 1975-10-21 | Atlantic Richfield Co | Catalytic oxidation of hydrocarbons with organic hydroperoxides |
| US3928452A (en) * | 1969-12-12 | 1975-12-23 | Rhone Poulenc Sa | Preparation of mixtures of ketones and of their corresponding alcohols |
| US4112004A (en) * | 1975-08-11 | 1978-09-05 | Toyo Soda Manufacturing Co., Ltd. | Process for producing alcohol |
| US4123616A (en) * | 1976-07-15 | 1978-10-31 | Toyo Soda Manufacturing Co., Ltd. | Process for hydrogenation of organic peroxide |
| US4219685A (en) * | 1979-04-20 | 1980-08-26 | Exxon Research & Engineering Co. | Improving odor of isopropanol |
| US4523928A (en) * | 1980-04-28 | 1985-06-18 | Battelle Development Corporation | Gasohol production from thermochemical conversion of biomass to ethanol |
| US4547598A (en) * | 1984-12-20 | 1985-10-15 | Texaco, Inc. | Cobalt borate catalyzed decomposition of organic hydroperoxides |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE637653A (en) * | 1963-09-19 |
-
1986
- 1986-06-27 US US06/879,660 patent/US4704482A/en not_active Expired - Lifetime
-
1987
- 1987-06-10 EP EP87305118A patent/EP0251526B1/en not_active Expired
- 1987-06-10 DE DE8787305118T patent/DE3766429D1/en not_active Expired - Fee Related
- 1987-06-25 JP JP62156717A patent/JP2504993B2/en not_active Expired - Lifetime
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2854487A (en) * | 1955-04-12 | 1958-09-30 | Distillers Co Yeast Ltd | Process for the manufacture of carbinols |
| US2993072A (en) * | 1956-06-15 | 1961-07-18 | Montedison Spa | Process for obtaining carboxylic acids from organic peroxides and carbon monoxide |
| US3360584A (en) * | 1965-05-25 | 1967-12-26 | Halcon International Inc | Process for the co-production of isoprene and oxygenated compounds from isopentane hydroperoxide |
| US3624165A (en) * | 1969-04-25 | 1971-11-30 | Monsanto Co | Purification process |
| US3928452A (en) * | 1969-12-12 | 1975-12-23 | Rhone Poulenc Sa | Preparation of mixtures of ketones and of their corresponding alcohols |
| US3914295A (en) * | 1972-12-18 | 1975-10-21 | Atlantic Richfield Co | Catalytic oxidation of hydrocarbons with organic hydroperoxides |
| US4112004A (en) * | 1975-08-11 | 1978-09-05 | Toyo Soda Manufacturing Co., Ltd. | Process for producing alcohol |
| US4123616A (en) * | 1976-07-15 | 1978-10-31 | Toyo Soda Manufacturing Co., Ltd. | Process for hydrogenation of organic peroxide |
| US4219685A (en) * | 1979-04-20 | 1980-08-26 | Exxon Research & Engineering Co. | Improving odor of isopropanol |
| US4523928A (en) * | 1980-04-28 | 1985-06-18 | Battelle Development Corporation | Gasohol production from thermochemical conversion of biomass to ethanol |
| US4547598A (en) * | 1984-12-20 | 1985-10-15 | Texaco, Inc. | Cobalt borate catalyzed decomposition of organic hydroperoxides |
Cited By (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5124492A (en) * | 1991-02-12 | 1992-06-23 | Uop | Process for decomposing peroxide impurities in a tertiary butyl alcohol feedstock using an iron (II) compound |
| US5196603A (en) * | 1991-02-12 | 1993-03-23 | Uop | Process for decomposing peroxide impurities in a teritary butyl alcohol feedstock using an iron (II) compound |
| EP0541312A1 (en) * | 1991-11-04 | 1993-05-12 | Texaco Chemical Company | Catalytic decomposition of impurities in methyl tertiary butyl ether |
| EP0555592A1 (en) * | 1992-02-10 | 1993-08-18 | Texaco Chemical Inc. | Catalytic decomposition of impurities in methyl tertiary butyl ether |
| US5741952A (en) * | 1992-02-10 | 1998-04-21 | Huntsman Specialty Chemicals Corporation | Catalytic decomposition of peroxides to purify a methyl tertiary butyl ether recycle stream |
| US5243101A (en) * | 1992-06-12 | 1993-09-07 | Texaco Chemical Company | Removal of peroxide contaminants from tertiary butyl alcohol |
| US5254759A (en) * | 1992-06-12 | 1993-10-19 | Texaco Chemical Company | Catalytic removal of peroxide contaminants from tertiary butyl alcohol |
| EP0581530A1 (en) * | 1992-07-28 | 1994-02-02 | Texaco Chemical Inc. | Catalytic removal of peroxide contaminants from a methanol-tertiary butyl alcohol recycle stream |
| EP0653406A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported rhodium catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653401A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported palladium, catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653402A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported lead oxide catalyst in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653404A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported chromium catalyst in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653407A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Conjoint production of ditertiary butyl peroxide and tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653405A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of supported palladium/platinum catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide |
| EP0653403A1 (en) * | 1993-11-12 | 1995-05-17 | Texaco Development Corporation | Use of titania or zirconia in the preparation of tertiary butyl alcohol from tertiary butyl alcohol from tertiary butyl hydroperoxide |
| US5583266A (en) * | 1994-05-02 | 1996-12-10 | Texaco Inc. | Integrated process for the production of isopropyl alcohol and diisopropyl ethers |
| US5436376A (en) * | 1994-08-11 | 1995-07-25 | Texaco Chemical Inc. | Production of tertiary butyl alcohol |
| EP0710640A1 (en) | 1994-11-01 | 1996-05-08 | Texaco Development Corporation | Recovery and purification of tertiary butyl alcohol |
| US5939592A (en) * | 1996-10-07 | 1999-08-17 | Huntsman Specialty Chemicals Corp. | Methods for decomposing esters and purifying alcohols |
| US6133484A (en) * | 1996-10-07 | 2000-10-17 | Huntsman Ici Chemical Llc | Methods for decomposing esters and purifying alcohols |
| WO1999024384A1 (en) * | 1997-11-10 | 1999-05-20 | Huntsman Specialty Chemicals Corporation | Methods for decomposing esters and purifying alcohols |
| US6037516A (en) * | 1997-11-20 | 2000-03-14 | Huntsman Ici Chemicals Llc | Method for removal of oxygenate impurities from organic chemical streams |
| US6613108B1 (en) * | 1998-10-16 | 2003-09-02 | Fortum Oil & Gas Oy | Process for producing a fuel component |
| US6518474B1 (en) | 1999-10-29 | 2003-02-11 | Huntsman International Llc | Process for producing isobutylene from tertiary butyl alcohol |
| WO2003048092A1 (en) | 2001-12-03 | 2003-06-12 | Arco Chemical Technology, L.P. | Purification of tertiary butyl alcohol |
| US20090269834A1 (en) * | 2008-04-25 | 2009-10-29 | Quinn Thomas J | Micro refinery system for ethanol production |
| CN111097510A (en) * | 2018-10-29 | 2020-05-05 | 中国石油化工股份有限公司 | TBA refined catalyst, preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0251526A2 (en) | 1988-01-07 |
| EP0251526A3 (en) | 1988-03-23 |
| EP0251526B1 (en) | 1990-11-28 |
| JPS638348A (en) | 1988-01-14 |
| JP2504993B2 (en) | 1996-06-05 |
| DE3766429D1 (en) | 1991-01-10 |
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